Use of salts as accelerators in an epoxy resin compound for chemical fastening

ABSTRACT

A method involves using at least one salt (S) selected from the salts of nitric acid, salts of nitrous acid, salts of halogens, or salts of trifluoromethanesulfonic acid, as an accelerator in a multi-component epoxy resin compound for the chemical fastening of construction elements and/or anchoring elements. Another method involves the chemical fastening of construction elements and anchoring elements, such as anchor rods, anchor bolts, rods, sleeves, reinforcing bars, screws, and the like in boreholes in various substrates.

The invention relates to the use of at least one salt (S) selected fromthe group consisting of salts of nitric acid, salts of nitrous acid,salts of halogens and salts of trifluoromethanesulfonic acid as anaccelerator in an epoxy resin compound for chemical fastening. Thepresent invention also relates to a method for the chemical fastening ofconstruction elements and anchoring means, such as anchor rods, anchorbolts, (threaded) rods, (threaded) sleeves, reinforcing bars, screws andthe like in boreholes in various substrates.

Multi-component mortar compounds based on curable epoxy resins and aminecuring agents have been known for some time and are used as adhesives,spackling pastes for repairing cracks and chemical anchors for fasteningconstruction elements such as anchor rods, reinforcing bars, and screwsin boreholes of various substrates. For use on outdoor constructionsites, the mortar compounds have to be easy to handle in a widetemperature range, and should only have low creep at elevatedtemperatures. At the same time, the mortar compounds should have a longprocessing time and should cure quickly and completely in a widetemperature range, and the cured mortar compounds should reach high loadvalues even with moist boreholes and high temperatures, and should havegood heat resistance.

These property profiles cannot be easily met. For instance, withconventional mortar compounds it is customary to provide a highproportion of low-viscosity constituents, a low filler proportion andcoarse fillers in order to achieve good handling behavior, although thisis disadvantageous in terms of low creep behavior under a load atelevated temperatures. In addition, a long processing time is achievedas a result of a high proportion of non-reactive or non-cross-linkingdiluents and less reactive components, and this prevents a short curingtime.

Mortar compounds based on epoxy amine also have slow curing kinetics, anextended pot life or gel time, and usually low heat resistance and creepresistance. This means that they can be handled easily and reach goodload values only in a narrow temperature range. The curing time ofmortar compounds based on epoxy amine is generally set by selecting anappropriate amine and/or by adding catalysts such as tertiary amines,alcohols and acids. However, these substances, which can be used asaccelerators, result in significant changes to the final properties ofthe cured mortar and often lead to problems with the properties relevantto the application. In particular, negative effects on the strength(load values) of the cured mortar can often be observed.

GB1105772 A describes the accelerating effect of inorganic metal saltson the reaction of epoxy resins with amines. As a rule, epoxy-aminesystems accelerated accordingly with inorganic salts are used ascoatings. This is described, for example, in

US2016/053108 A1, US2003/130481 A1 or U.S. Pat. No. 5,958,593.Compositions for use as coatings usually exhibit high mechanicalextensibility and are therefore unsuitable for chemical fastening.Mortar compounds for chemical fastening must have a high brittleness inorder to have the pull-out strength required for chemical fastening.

The problem addressed by the invention is therefore that of providing asolution for the chemical fastening of construction elements whichallows a considerable reduction in the curing time without impairing thepull-out strength of the mortar compound. In particular, the mortarcompounds should be able to withstand loads (90% of the reference load)within a time window of less than 7 hours, in particular less than 4hours, and should have excellent pull-out strength.

The problem addressed by the invention is solved by using a salt (S) asan accelerator in an epoxy resin compound for chemical fasteningaccording to claim 1. Preferred embodiments of the use according to theinvention are provided in the dependent claims, which may optionally becombined with one another.

The invention also relates to a method for the chemical fastening ofconstruction elements and/or anchoring means according to claim 12.Preferred embodiments of the use according to the invention are providedin the dependent claims, which may optionally be combined with oneanother.

Within the context of the invention, the terms used above and in thefollowing description have the following meanings:

-   -   “aliphatic compounds”are acyclic or cyclic, saturated or        unsaturated carbon compounds, excluding aromatic compounds;    -   “alicyclic compounds” are compounds having a carbocyclic ring        structure, excluding benzene derivatives or other aromatic        systems;    -   “araliphatic compounds” are aliphatic compounds having an        aromatic backbone such that, in the case of a functionalized        araliphatic compound, a functional group that is present is        bonded to the aliphatic rather than the aromatic part of the        compound;    -   “aromatic compounds” are compounds which follow Hackers rule        (4n+2);    -   “amines”are compounds which are derived from ammonia by        replacing one, two or three hydrogen atoms with hydrocarbon        groups, and have the general structures RNH₂ (primary amines),        R₂NH (secondary amines) and R₃N (tertiary amines) (see: IUPAC        Chemical Terminology, 2nd ed. (the “Gold Book”), compiled        by A. D. McNaught and A. Wilkinson, Blackwell Scientific        Publications, Oxford (1997)): and    -   “salts” are compounds that are made up of positively charged        ions (cations) and negatively charged ions (anions). There are        ionic bonds between these ions. The expression “salts of nitric        acid” describes compounds which are derived from nitric acid        (HNO₃) and which comprise a nitrate (NO₃ ⁻) as an anion. The        expression “salts of nitrous acid” describes compounds which are        derived from nitrous acid (HNO₂) and which comprise a nitrite        (NO₂ ⁻) as an anion. The expression “salts of halogens”        describes compounds which comprise an element from group 7 of        the periodic table as an anion. In particular, the expression        “salts of halogens” should be understood to mean compounds which        comprise a fluoride (F⁻), chloride (Cl⁻), bromide (Br⁻) or        iodide (I⁻) as an anion. The expression “salts of        trifluoromethanesulfonic acid” describes compounds which are        derived from trifluoromethanesulfonic acid (CF₃SO₃H) and which        comprise a triflate (CF₃SO₃) as an anion. In the context of the        present invention, the term “salt” also covers the corresponding        hydrates of the salts. The salts (S) used as accelerators are        also referred to as “salts” in the context of the present        invention.

It has now surprisingly been found that the addition of at least onesalt (S) to an epoxy resin compound for chemical fastening leads to aconsiderable acceleration of the curing reaction. The cured compoundsexhibit outstanding pull-out strength and can therefore be subjected toloading after only a short period of time, within approximately 4 to 6hours, and sometimes even much earlier, such as after less than 1 hour.Even when using amines that have very long curing times, only smallamounts of salt (S) are necessary to achieve excellent pull-outstrengths after a short time. Because even small amounts of the salt (S)are sufficient as an accelerator, the salt (S) itself has no negativeimpact on properties relevant to the application, such as therheological properties of the epoxy resin compound.

The epoxy resin compound is preferably used for construction purposes.The expression “for construction purposes” refers to the structuraladhesion of concrete/concrete, steel/concrete or steel/steel or one ofsaid materials with other mineral materials, to the structuralstrengthening of components made of concrete, brickwork and othermineral materials, to reinforcement applications with fiber-reinforcedpolymers of building objects, to the chemical fastening of surfaces madeof concrete, steel or other mineral materials, in particular thechemical fastening of construction elements and anchoring means, such asanchor rods, anchor bolts, (threaded) rods, (threaded) sleeves,reinforcing bars, screws and the like, in boreholes in varioussubstrates, such as (reinforced) concrete, brickwork, other mineralmaterials, metals (e.g. steel), ceramics, plastics, glass, and wood.

The epoxy resin compound is preferably a multi-component epoxy resincompound, preferably a two-component epoxy resin compound, whichcomprises an epoxy resin component (A) and a curing agent component (B).The epoxy resin component (A) comprises at least one curable epoxyresin. The curing agent component (B) comprises at least one amine whichis reactive to epoxy groups. In the multi-component epoxy resincompound, the epoxy resin component (A) and the curing agent component(B) are separate from one another so as to prevent a reaction. The salt(S) used as an accelerator can be contained in the epoxy resin component(A) or in the curing agent component (B) or in both the epoxy resincomponent (A) and the curing agent component (B). It is preferable forthe salt (S) to be contained at least in the curing agent component (B).The salt (S) is preferably contained in the curing agent component (B).

According to the invention, the salt (S) is at least one salt selectedfrom the group consisting of salts of nitric acid, salts of nitrousacid, salts of halogens, salts of trifluoromethanesulfonic acid andcombinations thereof. The salt (S) is preferably at least one saltselected from the group consisting of salts of nitric acid, salts ofhalogens, salts of trifluoromethanesulfonic acid and combinationsthereof. It has been found to be particularly preferable for the salt(S) to be selected from the group consisting of nitrates (NO₃ ⁻),iodides (I⁻), triflates (CF₃SO₃ ⁻) and combinations thereof.

Alkali metal nitrates, alkaline earth metal nitrates, lanthanidenitrates, aluminum nitrate, ammonium nitrate and mixtures thereof areparticularly suitable salts of nitric acid. Corresponding salts ofnitric acid are commercially available. Alkali metal nitrates and/oralkaline earth metal nitrates, such as Ca(NO₃)₂ or NaNO₃, are preferablyused as salts of nitric acid. It is also possible to use a solution of asalt in nitric acid as the salt (S), for example a solution containingCa(NO₃)₂/HNO₃. To prepare this solution, CaCO₃ is dissolved in HNO₃.

Alkali metal nitrites, alkaline earth metal nitrites, lanthanidenitrites, aluminum nitrite, ammonium nitrite and mixtures thereof areparticularly suitable salts of nitrous acid. Corresponding salts ofnitrous acid are commercially available. Alkali metal nitrites and/oralkaline earth metal nitrites, such as Ca(NO₂)₂, are preferably used assalts of nitrous acid.

Alkali metal halides, alkaline earth metal halides, lanthanide halides,aluminum halides, ammonium halides and mixtures thereof are particularlysuitable salts of halogens. Corresponding salts of halogens arecommercially available. The halogens are preferably selected from thegroup consisting of chloride, bromide, iodide and mixtures thereof, withiodides particularly preferably being used.

Alkali metal triflates, alkaline earth metal triflates, lanthanidetriflates, aluminum triflate, ammonium triflate and mixtures thereof areparticularly suitable salts of trifluoromethanesulfonic acid.Corresponding salts of trifluoromethanesulfonic acid are commerciallyavailable. Alkali metal nitrates and/or alkaline earth metal nitrates,such as Ca(CF₃SO₃)₂, are preferably used as salts oftrifluoromethanesulfonic acid.

In principle, the cations of the salt (S) can be organic, inorganic or amixture thereof. The cation of the salt (S) is preferably an inorganiccation.

Suitable organic cations are, for example, ammonium cations substitutedwith organic groups, such as C₁-C₆-alkyl groups, such astetraethylammonium cations.

Suitable inorganic cations of the salt (S) are preferably cationsselected from the group consisting of alkali metals, alkaline earthmetals, lanthanides, aluminum, ammonium (NH₄ ⁻) and mixtures thereof,more preferably from the group consisting of alkali metals, alkalineearth metals, aluminum, ammonium and mixtures thereof, and even morepreferably from the group consisting of alkali metals, alkaline earthmetals, aluminum and mixtures thereof. It is particularly preferable forthe cation of the salt (S) to be selected from the group consisting ofsodium, calcium, aluminum, ammonium and mixtures thereof.

The following compounds or components are therefore particularlysuitable as the salt (S): Ca(NO₃)₂ (calcium nitrate, usually used asCa(NO₃)₂ tetrahydrate), a mixture of Ca(NO₃)₂/HNO₃, KNO₃ (potassiumnitrate), NaNO₃ (sodium nitrate), Mg(NO₃)₂ (magnesium nitrate, usuallyused as Mg(NO₃)₂ hexahydrate), Al(NO₃)₃ (aluminum nitrate, usually usedas Al(NO₃)₃ nonahydrate), NH₄NO₃ (ammonium nitrate), Ca(NO₂)₂ (calciumnitrite), NaCl (sodium chloride), NaBr (sodium bromide), NaI (sodiumiodide), Ca(CF₃SO₃)₂ (calcium triflate), Mg(CF₃SO₃)₂ (magnesiumtriflate), and Li(CF₃SO₃)₂ (lithium triflate).

The epoxy resin component and/or the curing agent component can have oneor more salts (S). The salts can be used both individually and in amixture of two or more of the specified salts.

In order to improve the solubility properties of the salt (S) in theepoxy resin component and/or the curing agent component, the salt (S)can be dissolved in a suitable solvent and used accordingly as asolution. Organic solvents such as methanol, ethanol and glycerol, forexample, are suitable for this purpose. However, water can also be usedas the solvent, possibly also in a mixture with the above-mentionedorganic solvents. In order to prepare the corresponding salt solutions,the salt (S) is added to the solvent and stirred, preferably until it iscompletely dissolved.

The salt (S) is preferably contained in the epoxy resin compound in aproportion of from 0.1 to 4 wt. %, preferably 0.1 to 3 wt. %, based onthe total weight of the epoxy resin compound.

In the preferred embodiment in which the salt (S) is contained in thecuring agent component, this is preferably contained in the curing agentcomponent in a proportion of from 0.1 to 15 wt. %, based on the totalweight of the curing agent component. The salt (S) is preferablycontained in the curing agent component in a proportion of from 0.5 to12 wt. %, more preferably in a proportion of from 1.0 to 10 wt. %, evenmore preferably in a proportion of from 1.5 to 8.0 wt. %, based on thetotal weight of the curing agent component.

In the embodiment in which the salt (S) is contained in the epoxy resincomponent, this is preferably contained in the epoxy resin component ina proportion of from 0.1 to 5 wt. %, based on the total weight of theepoxy resin component. The salt (S) is preferably contained in the epoxyresin component in a proportion of from 0.5 to 4 wt. %, based on thetotal weight of the epoxy resin component.

The curing agent component (B) of the multi-component epoxy resincompound comprises, as the curing agent, at least one amine which isreactive to epoxy resins. The amine used as the curing agent is adiamine or polyamine selected from the group consisting of aliphatic,alicyclic, aromatic and araliphatic amines and has on average permolecule at least two reactive hydrogen atoms bonded to a nitrogen atom.The amine can be selected from the amines that are conventional forepoxy-amine systems and known to a person skilled in the art.

Examples of suitable amines are given below, without, howeverrestricting the scope of the invention:1,2-diaminoethane(ethylenediamine), 1,2-propanediamine,1,3-propanediamine, 1,4-diaminobutane, 2,2-dimethyl-1,3-propanediamine(neopentanediamine), diethylaminopropylamine (DEAPA),2-methyl-1,5-diaminopentane, 1,3-diaminopentane, 1,3-diaminopentane,2,2,4- or 2,4,4-trimethyl-1,6-diaminohexane and mixtures thereof (TMD),1,3-bis(aminomethyl)-cyclohexane (1,3-BAC),1,2-bis(aminomethyl)cyclohexane (1,2-BAC), hexamethylenediamine (HMD),1,2- and 1,4-diaminocyclohexane (1,2-DACH and 1,4-DACH),bis(4-aminocyclohexyl)methane (PACM),bis(4-amino-3-methylcyclohexyl)methane, diethylenetriamine (DETA),4-azaheptane-1,7-diamine, 1,11-diamino-3,6,9-trioxundecane,1,8-diamino-3,6-dioxaoctane, 1,5-diamino-methyl-3-azapentane,1,10-diamino-4,7-dioxadecane, bis(3-aminopropyl)amine,1,13-diamino-4,7,10-trioxatridecane, 4-aminomethyl-1,8-diaminooctane,2-butyl-2-ethyl-1,5-diaminopentane, N,N-bis(3-aminopropyl)methylamine,triethylenetetramine (TETA), tetraethylenepentamine (TEPA),pentaethylenehexamine (PEHA), 1,3-benzenedimethanamine(m-xylylenediamine, mXDA), 1,4-benzenedimethanamine (p-xylylenediamine,pXDA), 5-(aminomethyl)bicyclo[[2.2.1]hept-2-yl]methylamine (NBDA,norbornane diamine), dimethyldipropylenetriamine,dimethylaminopropylaminopropylamine (DMAPAPA),3-aminomethyl-3,5,5-trimethylcyclohexylamine (isophorone diamine(IPDA)), diaminodicyclohexyl methane (PACM), diethylmethylbenzenediamine(DETDA), 4,4′-diaminodiphenylsulfone (dapsone), mixed polycyclic amines(MPCA) (e.g. Ancamine 2168), dimethyldiaminodicyclohexylmethane (LarominC260), 2,2-bis(4-aminocyclohexyl)propane,(3(4),8(9)bis(aminomethyldicyclo[5.2.1.0^(2,6)]decane (mixture ofisomers, tricyclic primary amines; TCD-diamine), 4- methylcyclohexyldiamine (mCDA), N,N′-diaminopropyl-2-methyl-cyclohexane-1,3-diamine,N,N′-diaminopropyl-4-methyl-cyclohexane-1,3-diamine,N-(3-aminopropyl)cyclohexylamine, and2-(2,2,6,6-tetramethylpiperidin-4-yl)propane-1,3-diamine.

Preferred amines in the curing agent component are polyamines, such as2-methylpentanediamine (DYTEK A),3-aminomethyl-3,5,5-trimethylcyclohexane (IPDA),1,3-benzenedimethanamine (m-xylylenediamine, mXDA),4,4′-methylenebis(cyclohexyl-amine) (PACM), 1,4-benzenedimethanamine(p-xylylenediamine, PXDA), 1,6-diamino-2,2,4-trimethylhexane (TMD),diethylenetriamine (DETA), triethylenetetramine (TETA),tetraethylenepentamine (TEPA), pentaethylenehexamine (PEHA),N-ethylaminopiperazine (N-EAP),(3(4),8(9)bis(aminomethyl)dicyclo[5.2.1.0^(2,6)]decane (mixture ofisomers, tricyclic primary amines; TCD-diamine),1,14-diamino-4,11-dioxatetradecane, dipropylenetriamine,2-methyl-1,5-pentanediamine, N,N′-dicyclohexyl-1,6-hexanediamine,N,N′-dimethyl-1,3-diaminopropane, N,N′-diethyl-1,3-diaminopropane,N,N-dimethyl-1,3-diaminopropane, secondary polyoxypropylenedi- andtriamines, 2,5-diamino-2,5-dimethylhexane,bis(amino-methyl)tricyclopentadiene, 1,8-diamino-p-menthane,bis(4-amino-3,5-dimethylcyclohexyl)methane,1,3-bis(aminomethyl)cyclohexane (1,3-BAC),1,2-bis(aminomethyl)cyclohexane (1,2-BAC), dipentylamine,N-2-(aminoethyl)piperazine (N-AEP), N-3-(aminopropyl)piperazine,piperazine and methylcyclohexyl diamine (mCDA),N,N′-diaminopropyl-2-methyl-cyclohexane-1,3-diamine,N,N′-diaminopropyl-4-methyl-cyclohexane-1,3-diamine,N-(3-aminopropyl)cyclohexylamine, and2-(2,2,6,6-tetramethylpiperidin-4-yl)propane-1,3-diamine.

The amine reactive to epoxy groups is preferably selected from3-aminomethyl-3,5,5-trimethylcyclohexane (IPDA),2-methyl-1,5-pentanediamine (DYTEK A), m-xylylenediamine (mXDA),1,3-bis(aminomethyl)-cyclohexane (1,3-BAC),1,2-bis(aminomethyl)cyclohexane (1,2-BAC), 4,4′-methylenebis(cyclohexyl-amine) (PACM), 4-methylcyclohexyl-diamine(mCDA) and mixtures thereof. In particular, the salt (S) is used in acuring agent component which comprisesaminomethyl-3,5,5-trimethylcyclohexane.

The amines can be used both individually and in a mixture of two or moreof the specified amines.

The amine which is reactive to epoxy groups is preferably contained inthe curing agent component in a proportion of from 10 to 90 wt. %,particularly preferably from 35 to 60 wt. %, based on the total weightof the curing agent component.

The curing agent component can comprise further additives from the groupof solvents, further phenolic accelerants, co-accelerants, adhesionpromoters and inorganic fillers.

Non-reactive diluents (solvents) may preferably be contained in amountof up to 30 wt. %, based on the total weight of the curing agentcomponent, for example from 1 to 20 wt. %. Examples of suitable solventsare alcohols, such as methanol, ethanol or glycols, lower alkyl ketonessuch as acetone, di lower alkyl lower alkanoyl amides such asdimethylacetamide, lower alkyl benzenes such as xylenes or toluene,phthalic acid esters or paraffins. The amount of solvents is preferably5 5 wt. %, based on the total weight of the curing agent component.

The phenolic accelerants are preferably selected from salicylic acid,styrenated phenols and cardanol, and mixtures thereof. These may bepresent in the curing agent component in a proportion of from 0 to 10wt. %, based on the total weight of the curing agent component.

Benzene alcohol, tertiary amines, novolac resins, imidazoles or tertiaryaminophenols, organophosphines, Lewis bases or acids such as phosphoricacid esters, or mixtures of two or more thereof, can be used asco-accelerators, for example. The co-accelerators are preferablycontained in the curing agent component in a weight proportion of from0.001 to 5 wt. %, based on the total weight of the curing agentcomponent.

Examples of suitable co-accelerators are in particulartris-2,4,6-dimethylaminomethylphenol, 2,4,6-tris(dimethylamino)phenoland bis[(dimethylamino)methyl]phenol. A suitable co-accelerator mixturecontains 2,4,6-tris(dimethylaminomethyl)phenol andbis(dimethylaminomethyl)phenol. Mixtures of this kind are commerciallyavailable, for example as Ancamine® K54 (Evonik, Germany).

By using an adhesion promoter, the cross-linking of the borehole wallwith the mortar compound is improved such that the adhesion increases inthe cured state. Suitable adhesion promoters are selected from the groupof silanes that have at least one Si-bound hydrolyzable group, such as3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane,2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane,N-2-(aminoethyl)-3-aminopropylmethyl-diethoxysilane,N-2-(aminoethyl)-3-aminopropyl-5 triethoxysilane,3-aminopropyl-trimethoxysilane, 3-aminopropyltriethoxysilane,N-phenyl-3-aminoethyl-3-aminopropyl-trimethoxysilane,3-mercaptopropyltrimethoxysilane and3-mercaptopropylmethyldimethoxysilane. In particular,3-aminopropyl-trimethoxysilane (AMMO), 3-aminopropyltriethoxysilane(AMEO), 2-aminoethyl-3-aminopropyl-trimethoxysilane (DAMO) andtrimethoxysilylpropyldiethylenetetramine (TRIAMO) are preferred asadhesion promoters. Further silanes are described, for example, inEP3000792 A1, the content of which is hereby incorporated in the presentapplication.

The adhesion promoter can be contained in an amount of up to 10 wt. %,preferably from 0.1 to 5 wt. %, more preferably from 1.0 to 2.5 wt. %,based on the total weight of the curing agent component.

Inorganic fillers, in particular cements such as Portland cement oraluminate cement and other hydraulically setting inorganic substances,quartz, glass, corundum, porcelain, earthenware, baryte, light spar,gypsum, talc and/or chalk and mixtures thereof are used as fillers. Inaddition, thickeners such as fumed silica can also be used as aninorganic filler. Particularly suitable fillers are quartz powders, finequartz powders and ultra-fine quartz powders that have not beensurface-treated, such as Millisil W3, Millisil W6, Millisil W8 andMillisil W12, preferably Millisil W12. Silanized quartz powders, finequartz powders and ultra-fine quartz powders can also be used. These arecommercially available, for example, from the Silbond product seriesfrom Quarzwerke. The product series Silbond EST (modified withepoxysilane) and Silbond AST (treated with aminosilane) are particularlypreferred. Furthermore, it is possible for fillers based on aluminumoxide such as aluminum oxide ultra-fine fillers of the ASFP type fromDenka, Japan (d₅₀=0.3 μm) or grades such as DAW or DAM with the typedesignations 45 (d₅₀<0.44 μm), 07 (d₅₀>8.4 μm), 05 (d₅₀<5.5 μm) and 03(d₅₀<4.1 μm). Moreover surface-treated fine and ultra-fine fillers ofthe Aktisil AM type (treated with aminosilane, d₅₀=2.2 μm) and AktisilEM (treated with epoxysilane, d50=2.2 μm) from Hoffman Mineral can beused.

The inorganic fillers can be added in the form of sands, flours, ormolded bodies, preferably in the form of fibers or balls. The fillersmay also be present in one or all components of the multi-componentmortar compound. A suitable selection of the fillers with regard to typeand particle size distribution/(fiber) length can be used to controlproperties relevant to the application, such as rheological behavior,press-out forces, internal strength, tensile strength, pull-out forcesand impact strength.

The proportion of fillers is preferably from 0 to 75 wt. %, for examplefrom 10 to 75 wt. %, preferably from 15 to 75 wt. %, more preferablyfrom 20 to 50 wt. %, and even more preferably from 25 to 40 wt. %, basedon the total weight of the curing agent component.

The epoxy resin component (A) preferably comprises at least one curableepoxy resin. A large number of the compounds known to a person skilledin the art and commercially available for this purpose, which contain onaverage more than one epoxy group, preferably two epoxy groups, permolecule can be used as a curable epoxy in the epoxy resin component(A). These epoxy resins may be both saturated and unsaturated as well asaliphatic, alicyclic, aromatic or heterocyclic, and may also havehydroxyl groups. They may also contain substituents which do not causedisruptive secondary reactions under the mixing or reaction conditions,for example alkyl or aryl substituents, ether groups and the like.Trimeric and tetrameric epoxies are also suitable in the context of theinvention.

The epoxy resins are preferably glycidyl ethers which are derived frompolyhydric alcohols, in particular from polyhydric phenols such asbisphenols and novolacs, in particular those having an average glycidylgroup functionality of 1.5 or greater, in particular 2 or greater, forexample from 2 to 10.

The epoxy resins can have an epoxy equivalent weight (EEW) of from 120to 2000 g/EQ, preferably from 140 to 400, in particular from 155 to 195,for example from 165 to 185. Mixtures of a plurality of epoxy resins mayalso be used.

Examples of the polyhydric phenols used to prepare the epoxy resins areresorcinol, hydroquinone, 2,2-bis-(4-hydroxyphenyl)propane (bisphenolA), isomer mixtures of dihydroxyphenylmethane (bisphenol F),tetrabromobisphenol A, novolacs, 4,4′-dihydroxyphenylcyclohexane and4,4′-dihydroxy-3,3′-dimethyldiphenylpropane.

The epoxy resin is preferably a diglycidyl ether of bisphenol A orbisphenol F or a mixture thereof. Liquid diglycidyl ethers based onbisphenol A and/or F having an EEW of from 180 to 190 g/EQ areparticularly preferably used.

Further examples are hexanediol diglycidyl ether, trimethylolpropanetriglycidyl ether, bisphenol A epichlorohydrin resins and/or bisphenol Fepichlorohydrin resins, for example having an average molecular weightof Mn≤2000 g/mol.

The proportion of epoxy resin is >0 to 100 wt. %, preferably 10 to 70wt. % and particularly preferably 30 to 60 wt. %, based on the totalweight of the epoxy resin component (A).

In addition to the epoxy resins, the epoxy resin component (A) mayoptionally contain at least one reactive diluent. Glycidyl ethers ofaliphatic, alicyclic or aromatic monoalcohols or in particularpolyalcohols having a lower viscosity than epoxies containing aromaticgroups are used as reactive diluents. Examples of reactive diluents aremonoglycidyl ethers, e.g. o-cresyl glycidyl ether, and glycidyl ethershaving an epoxy functionality of at least 2, such as 1,4-butanedioldiglycidyl ether (BDDGE), cyclohexanedimethanol diglycidyl ether andhexanediol diglycidyl ether, as well as tri- or higher glycidyl ethers,such as glycerol triglycidyl ether, pentaerythritol tetraglycidyl ether,trimethylolpropane triglycidyl ether (TMPTGE), or trimethylolethanetriglycidyl ether (TMETGE), with trimethylolethane triglycidyl etherbeing preferred. Mixtures of two or more of these reactive diluents canalso be used, preferably mixtures containing triglycidyl ethers,particularly preferably as a mixture of 1,4-butanediol diglycidyl ether(BDDGE) and trimethylolpropane triglycidyl ether (TMPTGE) or1,4-butanediol diglycidyl ether (BDDGE) and trimethylolethanetriglycidyl ether (TMETGE).

The reactive diluents are preferably present in an amount of from 0 to60 wt. %, in particular from 1 to 20 wt. %, based on the total weight ofthe resin component (A).

The proportion of the epoxy component (A) in the total mass of themulti-component mortar compound is preferably 5 to 90 wt %, inparticular 20 to 80 wt. %, 30 to 70 wt. % or 40 to 60 wt. %.

Suitable epoxy resins and reactive diluents can also be found in thestandard reference from Michael Dornbusch, Ulrich Christ and Rob Rasing,“Epoxidharze,” Vincentz Network GmbH & Co. KG (2015), ISBN 13:9783866308770. These compounds are included here by reference.

Furthermore, the epoxy resin component (A) can contain conventionaladditives, in particular adhesion promoters and fillers, as alreadydescribed for the curing agent component.

The adhesion promoter can be contained in an amount of up to 10 wt. %,preferably from 0.1 to 5 wt. %, particularly preferably from 1.0 to 5.0wt. %, based on the total weight of the epoxy resin component (A).

The proportion of fillers is preferably from 0 to 75 wt. %, for examplefrom 10 to 75 wt. %, preferably from 15 to 75 wt. %, more preferablyfrom 20 to 50 wt. %, and even more preferably from 25 to 40 wt. %, basedon the total weight of the epoxy resin component (A).

Further conceivable additives to the multi-component epoxy resincompound are also thixotropic agents such as optionally organicallyafter-treated fumed silica, bentonites, alkyl- and methylcelluloses andcastor oil derivatives, plasticizers such as phthalic or sebacic acidesters, stabilizers, antistatic agents, thickeners, flexibilizers,curing catalysts, rheology aids, wetting agents, coloring additives suchas dyes or pigments, for example for different staining of componentsfor improved control of their mixing, as well as wetting agents,desensitizing agents, dispersants and other control agents for thereaction rate, or mixtures of two or more thereof.

The multi-component epoxy resin compound is preferably present incartridges or film pouches which comprise two or more separate chambersin which the epoxy resin component (A) and the curing agent component(B) of the mortar compound are separately arranged so as to prevent areaction.

In the use as intended, the epoxy resin component (A) and the curingagent component (B) are discharged out of the separate chambers andmixed in a suitable device, for example a static mixer or dissolver. Themixture of epoxy resin component (A) and curing agent component (B) isthen introduced into the previously cleaned borehole by means of a knowninjection device. The component to be fastened is then inserted into themortar compound and aligned. The reactive constituents of the curingagent component (B) react with the epoxy resin of the resin component(A) by polyaddition such that the epoxy resin compound cures underenvironmental conditions within a desired period of time, preferablywithin minutes or hours.

Components A and B are preferably mixed in a ratio that results in abalanced stoichiometry according to the EEW and AHEW values.

The AHEW value (amine hydrogen equivalent weight, H equivalent) providesthe amount of the curing agent component which contains 1 mol ofreactive H. The ANEW is determined in a manner known to a person skilledin the art on the basis of the formulation of the reaction mixture fromthe known H equivalents of the used reactants and raw materials fromwhich they are calculated.

Using the example of meta-xylylenediamine (M_(w)=136 g/mol,functionality=4 eq/mol), the calculation of the AHEW is explained belowby way of example:

${{General}{formula}:{AHEW}} = {\frac{Mw}{Functionality} = {{\frac{136}{4}\left\lbrack \frac{g}{eq} \right\rbrack} = {34\left\lbrack \frac{g}{eq} \right\rbrack}}}$

The EEW (epoxide equivalent weight, epoxide equivalent values) aregenerally provided by the manufacturers of the epoxy resin componentsused in each case or are calculated according to known methods. The EEWvalues provide the amount in g of epoxy resin which contains 1 mol ofepoxy groups.

Experimentally, the AHEW was obtained by determining the glasstransition temperature (Tg) from a mixture of epoxy resin (with knownEEW) and an amine component. In this case, the glass transitiontemperatures of epoxy resin/amine mixtures were determined withdifferent ratios. The sample was cooled at a heating rate of −20 K/minfrom 21 to −70° C., heated in a first heating cycle to 250° C. (heatingrate 10 K/min), then re-cooled to −70° C. (heating rate −20 K/min) andheated (20 K/min) to 200° C. in the last step. The mixture having thehighest glass transition temperature in the second heating cycle(“T_(g)2”) has the optimum ratio of epoxy resin and amine. The AHEWvalue can be calculated from the known EEW and the optimum epoxyresin/amine ratio.

Example: EEW=158 g/mol

Amine/epoxy resin mixture having a maximum Tg2: 1 g amine with 4.65 gepoxy resin

${AHEW} = {{\frac{1}{4.65} \cdot 158} = {34\left\lbrack \frac{g}{eq} \right\rbrack}}$

The present invention also relates to a method for the chemicalfastening of construction elements and/or anchoring means in boreholes,a multi-component epoxy resin compound as described above being used forthe chemical fastening of the construction elements. The methodaccording to the invention is particularly suitable for the structuraladhesion of concrete/concrete, steel/concrete or steel/steel or one ofsaid materials with other mineral materials, for the structuralstrengthening of components made of concrete, brickwork and othermineral materials, for reinforcement applications with fiber-reinforcedpolymers of building objects, for the chemical fastening of surfacesmade of concrete, steel or other mineral materials, in particular thechemical fastening of construction elements and anchoring means, such asanchor rods, anchor bolts, (threaded) rods, (threaded) sleeves,reinforcing bars, screws and the like, in boreholes in varioussubstrates, such as (reinforced) concrete, brickwork, other mineralmaterials, metals (e.g. steel), ceramics, plastics, glass, and wood. Themethod according to the invention is very particularly preferably usedfor the chemical fastening of anchoring means.

Where applicable, the above statements regarding the use according tothe invention apply equally to the method according to the invention.

Further advantages of the invention can be found in the followingdescription of preferred embodiments, which are not understood to be inany way limiting, however. All embodiments of the invention can becombined with one another within the scope of the invention.

EXAMPLES

The chemicals listed in table 1 below have been used to illustrate theexamples:

TABLE 1 List of chemicals used Substance Trade name CAS numberManufacturer Country 1,2,3-propanetriol Glycerol 56-81-5 Merck G1,2-diaminocyclohexane Dytek DCH-99 694-83-7 Invista NL1,3-cyclohexanedimethanamine 1,3-BAC 2579-20-6 Itochu G Deutschland1,3-dihydroxybenzene Resorcinol 108-46-3 Sigma-Aldrich G 2,4,6- AncamineK54 90-72-2, Air Products NL tris(dimethylaminomethyl)phenol, 71074-89-0bis[(dimethylamino)methyl]phenol 2-methyl-1,5-pentamethylene Dytek A15520-10-2 Invista NL diamine 4,4′-methylenebis(2-methyl- MACM 6864-37-5Sigma-Aldrich G cyclohexylamine) Aluminum nitrate nonahydrate Aluminumnitrate 7784-27-2 Sigma-Aldrich G Ammonium nitrate Ammonium nitrate6484-52-2 Sigma-Aldrich G Calcium carbonate Calcium carbonate 471-34-1Sigma-Aldrich G Calcium nitrate tetrahydrate Calcium nitrate 13477-34-4Sigma-Aldrich G Calcium nitrite solution, 30% Calcium nitrite 13780-06-8Sigma-Aldrich G solution, 30% in water Calcium oxide Calcium oxide1305-78-8 Sigma-Aldrich G Calcium propionate Calcium propionate4075-81-4 Sigma-Aldrich G Calcium sulfate dihydrate Calcium sulfate10101-41-1 Hilliges G dihydrate 75 Gipswerk Calciumtrifluoromethanesulfonate Calcium triflate 55120-75-7 Sigma-Aldrich GIsophorone diamine Vestamin IPD 2855-13-2 Evonik G Degussa Potassiumnitrate Potassium nitrate 7757-79-1 Sigma-Aldrich G Potassium sulfatePotassium sulfate 7778-80-5 Sigma-Aldrich G Lithium hydroxide Lithiumhydroxide 1310-65-2 Sigma-Aldrich G Lithium trifluoromethanesulfonateLithium triflate 33454-82-9 TCI Europe B Magnesium nitrate Magnesiumnitrate 13446-18-9 Sigma-Aldrich G hexahydrate Magnesium Magnesiumtriflate 60871-83-2 Alfa Aesar G trifluoromethanesulfonatem-Xylylenediamine mXDA 1477-55-0 Itochu G Deutschland Sodium bromideSodium bromide 7647-15-6 Sigma-Aldrich G Sodium chloride Sodium chloride7647-14-5 VWR Prolabo G Sodium iodide Sodium iodide 7681-82-5Sigma-Aldrich G Sodium nitrate Chile-Salpeter 7631-99-4 Sigma-Aldrich G4-hydroxyphenylacetic acid 4-hydroxyphenylacetic 156-38-7 TCI Europe Bacid Phenol novolac resin Phenolite TD-2131 9003-35-4 DIC Europe Gp-Toluenesulfonic acid p-Toluenesulfonic acid 6192-52-5 TCI Europe Bmonohydrate Salicylic acid Salicylic acid 69-72-7 Merck G Nitric acid70% Nitric acid 7697-37-2 Sigma-Aldrich G Styrenated phenol Novares LS500 61788-44-1 Rütgers G Novares GmbH Tetrabutylammonium nitrateTetrabutylammonium 1941-27-1 Sigma-Aldrich G nitrate Trifluoroaceticacid Trifluoroacetic acid 76-05-1 TCI Europe B

1. Determination of the Reaction Kinetics by Temperature MeasurementEpoxy Resin Component (A)

In the examples, the bisphenol A-based and bisphenol F-based epoxyresins commercially available under the names Araldite GY 240 andAraldite GY 282 (Huntsman), respectively, were used as the epoxy resins.

The 1,4-butanediol-diglycidyl ether and trimethyolpropane-triglycidylether commercially available under the names Araldite DY-026 andAraldite™ DY-T (Huntsman), respectively, were used as the reactivediluents.

An epoxy resin component (A) composed as specified in table 2 below wasprepared. The components were mixed and stirred in the dissolver (PClaboratory system, volume 1 L) at a negative pressure of 80 mbar for 10minutes at 3500 rpm.

TABLE 2 Composition of epoxy resin component (A) Substance FunctionPercent by weight Bisphenol A-based epoxy resin Epoxy resin  52Bisphenol F-based epoxy resin Epoxy resin  28 1,4-butanediol-diglycidylether Reactive diluent  10 Trimethylolpropane triglycidyl ether Reactivediluent  10 EEW [g/Eq] 158

Curing Agent Component (B)

The amine isophorone diamine (IPDA, trade name Vestamin IPD) from EvonikDegussa, Germany was used as the curing agent component (B). To preparethe curing agent component (B), the amount of salt (S) specified intable 3 was added to IPDA and dissolved as far as possible. This mixturewas used as the curing agent component. The mixing ratios werecalculated based on the ANEW content of IPDA (42.6 g/EQ), theaccelerator content and the EEW content of the epoxy resin component(A).

To determine the reaction kinetics by temperature measurement, the epoxyresin component (A) together with the curing agent component was pouredinto a 20-ml rolled-rim glass. A temperature sensor was placed in thecenter of the rolled-rim glass. The temperature change was recorded(device: Yokogawa, DAQ station, model: DX1006-3-4-2). With this method,the curing of the mortar could be followed over the course of thetemperature development. If there was an acceleration during curing, themaximum temperature is shifted to shorter times, associated with ahigher temperature. T_(max) (maximum temperature reached) and t_(Tmax)(time after which the maximum temperature was reached) were measured.

The results of the determination of the reaction kinetics by temperaturemeasurement for different salts (S) as accelerators are shown in table 3below.

TABLE 3 Results of the determination of the reaction kinetics ProportionT_(max) t_(max) Salt (S) [wt. %] [° C.] [hh:mm:ss] Calcium nitratetetrahydrate 2 193 00:29:13 5 189 00:12:34 Calcium nitratetetrahydrate/Ancamin K54 2/2 85 00:19:05 Cacium nitratetetrahydrate/Calcium triflate/ 2/2/2 111 00:07:34 Ancamin K54 Calciumnitrate/nitric acid solution 2 159 00:20:26 5 176 00:09:32 Potassiumnitrate (25.0% in H₂O) 8 153.2 00:43:50 20 145.8 00:19:25 Sodium nitrate(46.6% in H₂O) 4.3 125.2 01:10:58 10.7 135.1 00:38:06 Magnesium nitratehexahydrate 2 36 01:12:52 5 152 00:38:21 Aluminum nitrate nonahydrate 255 01:11:33 5 169 00:38:52 Ammonium nitrate 2 173.3 00:39:11 5 195.900:19:40 Calcium nitrite (30.0% in H₂O) 6.7 207 00:12:53 16.7 164.700:06:41 Sodium chloride (26.4% in H₂O) 7.6 130 00:43:56 18.9 157.700:27:29 Sodium bromide (47.56% in H₂O) 4.2 157.2 00:47:22 10.5 145.800:29:37 Sodium iodide 2 135 01:13:03 5 152 00:24:46 Calcium triflate 2212 00:21:49 5 230 00:07:05 Calcium triflate/Ancamine K54 2.2 14100:16:53 Magnesium triflate 2 46.2 02:34:25 5 100.5 01:35:59 Lithiumtriflate 2 183.5 00:34:48 5 222.6 00:14:56

For comparison, the reaction kinetics by temperature measurement werecarried out for numerous accelerators which are known from the priorart. The results of this measurement are shown in table 4 below.

TABLE 4 Results of the determination of the reaction kinetics bytemperature measurement for different accelerators (comparativeexamples) Concentration T_(max) t_(max) Accelerator [wt. %] [° C.][hh:mm:ss] — 36.8 02:17:03 H₂O 5 65.5 01:18:12 10 86.8 00:36:45Resorcinol 10 81 01:18:20 20 172 00:27:48 Glycerol 5 24 04:55:38 10 3202:15:26 Calcium oxide 2 23 05:04:05 5 27 00:51:02 Phenolacetic acid 528 00:23:14 10 23 00:16:37 Styrenated phenol ‘LS 500’ 10 27 03:06:47 2029 02:28:30 p-Toluenesulfonic acid 2 26 03:02:25 5 25 03:04:48 AncaminK54 2 25 03:57:52 5 24 05:34:45 Salicylic acid 2 32 01:16:25 5 3601:30:38 Phenolite TD-2131 15 165 00:54:23 25 147 00:38:37Trifluoroacetic acid 2 31 01:47:13 5 73 01:22:20 Lithium hydroxide 2 2300:17:00 5 23 05:21:27 Potassium sulfate 2 45.4 03:07:59 5 46.8 02:29:52Calcium sulfate 2 25 05:14:48 5 24 04:41:34 Calcium propionate 2 36.503:26:25 5 41.5 03:22:06 Tetrabutylammonium nitrate 2 43 02:21:04 5 3802:27:56 Potassium sulfate 20.0 136.9 00:17:50 (10.02% in H₂O) 49.9 98.200:12:12

Variation of the Amine in the Curing Agent Component

The curing agent component (B) was modified in that the amine IPDA wasreplaced by the amines listed in table 5 below and combined with thesalts (S) specified in each case. The results of the determination ofthe reaction kinetics by temperature measurement are given in tables 5(according to the invention) and 6 (comparative examples) below.

TABLE 5 Results of the determination of the reaction kinetics bytemperature measurement with variation of the amine in the curing agentcomponent Proportion T_(max) t_(max) Amine Salt (S) [wt. %] [° C.][hh:mm:ss] 1,3-BAC Calcium nitrate 2 165 00:11:45 tetrahydrate 1,3-BACCalcium nitrate 2.5 257.5 00:13:20 tetrahydrate in glycerol (80%solution) MACM Calcium nitrate 2 61 00:55:29 tetrahydrate Dytek ACalcium nitrate 2.5 226.5 00:15:32 tetrahydrate in glycerol (80%solution) 1,2-BAC Calcium triflate 2 146.5 01:14:13 mXDA Sodium iodidein 5.5 239.0 00:40:52 glycerol (36.4% solution)

TABLE 6 Results of the determination of the reaction kinetics bytemperature measurement with variation of the amine in the curing agentcomponent using a novolac accelerator Concentration Tmax tmax AminesAccelerator [%] [° C.] [hh:mm:ss] 1,3-BAC — 33 03:08:35 MACM — 2203:12:37 MACM Phenolite TD-2131 15 50 01:20:40 Dytek A Phenolite TD-213115 222.7 00:33:17 1,2-BAC Phenolite TD-2131 15 57.1 01:25:53 1,3-BACPhenolite TD-2131 15 209.5 00:25:07 mXDA Phenolite TD-2131 15 224.900:38:46

2. Mortar Compounds and Pull-Out Tests Epoxy Resin Component (A)

In the examples, the bisphenol A-based and bisphenol F-based epoxyresins commercially available under the names Araldite GY 240 andAraldite GY 282 (Huntsman), respectively, were used as the epoxy resins.

The 1,4-butanediol-diglycidyl ether and trimethyolpropane-triglycidylether commercially available under the names Araldite DY-026 andAraldite™ DY-T (Huntsman), respectively, were used as the reactivediluents.

3-glycidyloxypropyl-trimethoxysysilane available under the nameDynalsylan GLYMO™ (Evonik Industries) was used as the adhesion promoter.

The liquid components were premixed by hand. Subsequently, quartz(Millisil™ W12 from Quarzwerke Frechen) was added as a filler and fumedsilica (Cab-O-SiI™ TS-720 from Cabot Rheinfelden) was added as athickener and the mixture was stirred in the dissolver (PC laboratorysystem, volume 1 L) for 10 minutes at a negative pressure of 80 mbar at3500 rpm.

The composition of the epoxy resin component (A) used in the examples isgiven in table 7 below.

TABLE 7 Composition of the epoxy resin component (A) in wt. % Percent byweight Substance Function [wt. %] 3-glycidyloxypropyl-trimethoxysysilaneAdhesion promoter 2.8 Bisphenol A-based epoxy resin Epoxy resin 31.3Bisphenol F-based epoxy resin Epoxy resin 16.9 1,4-butanediol-diglycidylether Reactive diluent 6.0 Trimethyolpropane-triglycidyl ether Reactivediluent 6.0 Quartz Filler 34.4 Silicic acid Thickener 2.7 EEW [g/Eq] 255

Curing Agent Component (B) Starting Materials

Isophorone diamine (IPDA) from Evonik Degussa, Germany,1,3-cyclohexanedimethanamine (1,3-BAC) and m-xylylenediamine (mXDA) fromMGC, Japan and 2-methlypentamethylenediamine (Dytek A) from Invista, theNetherlands, were used as amines for preparing the curing agentcomponent (B).

Quartz (Millisil™ W12 from Quarzwerke Frechen) and calcium aluminatecement (Secar 80 from Kerneos SA) were used as a filler and fumed silica(Cab-O-SiI™ TS-720 from Cabot Rheinfelden) was used as a thickener.

The salts calcium nitrate and sodium iodide were used as solutions inglycerol (1,2,3-propanetriol, CAS No. 56-81-5, Merck, G). To prepare thecalcium nitrate solution, 400.0 g calcium nitrate tetrahydrate was addedto 100.0 g glycerol and stirred at 50° C. until completely dissolved(approx. 3 hours). The solution prepared in this way contained 80.0%calcium nitrate tetrahydrate. To prepare the sodium iodide solution,36.4 g sodium iodide was added to 63.6 glycerol and stirred at 50° C.until completely dissolved. The solution prepared in this way contained36.4% sodium iodide.

Calcium triflate was dissolved as a solid in the amine of the particularcuring agent.

A calcium nitrate/nitric acid solution was also used as the salt (S). Toprepare this solution, 52.6 g calcium carbonate was slowly added to135.2 g nitric acid and then stirred for 5 minutes.

The liquid components were mixed to prepare the curing agent components(B). The accelerator was added and quartz powder and silicic acid werethen added and stirred in the dissolver (PC laboratory system, volume1L) for 10 minutes at a negative pressure of 80 mbar at 2500 rpm.

The composition of the curing agent components (B) prepared in this wayis specified in tables 8 (according to the invention) and 9 (comparativeexamples) below:

TABLE 8 Composition of the curing agent component (B) in wt. % Example 12 3 4 Amine 1,3-BAC 36.75 — — — mXDA — 41.2 — — IPDA — — 42.0 — DYTEK A— — — 42.0 Accelerator Sodium iodide 8.25 — — — Calcium nitrate — 3.8 —— Calcium nitrate/nitric acid — — 3.0 — Calcium triflate — — — 3.0Quartz 25.0 25.0 25.0 25.0 Calcium aluminate cement 25.0 25.0 25.0 25.0Thickener 5.0 5.0 5.0 5.0 AHEW [g/Eq] 97 83 101 69

TABLE 9 Composition of the curing agent component (B) of comparativeexamples 1 to 5 in wt. % Example 1 2 3 4 5 Amine 1,3-BAC 36.6 — — — —mXDA — 36.6 — — — IPDA — — 27.6 36.6 — DYTEK A — — — — 36.6 AcceleratorPhenolite TD-2131 6.0 6.0 — 6.0 6.0 Ancamine K54 2.4 2.4 2.4 2.4 2.4Novares LS 500 — — 15.0 — — Quartz 25.0 25.0 25.0 25.0 25.0 Calciumaluminate cement 25.0 25.0 25.0 25.0 25.0 Thickener 5.0 5.0 5.0 5.0 5.0AHEW [g/Eq] 97 93 154 116 79

Mortar Compounds and Pull-Out Tests

The epoxy resin component (A) and the curing agent component (B) weremixed in a speed mixer in a ratio resulting in a balanced stoichiometryaccording to the EEW and AHEW values. The mixture was poured into aone-component cartridge as far as possible without bubbles, and wasimmediately injected into the borehole made for the pull-out tests.

The pull-out strength of the mortar compounds obtained by mixing theepoxy resin component (A) and the curing agent component (B) accordingto the above examples was determined using a high-strength threadedanchor rod M12 according to ETAG 001 Part 5, which was doweled into ahammer-drilled borehole having a diameter of 14 mm and a borehole depthof 69 mm with the relevant mortar compound in C20/25 concrete. Theboreholes were cleaned by means of compressed air (2×6 bar), a wirebrush (2×) and again by compressed air (2×6 bar).

The boreholes were filled up, by two thirds from the bottom of theborehole, with the mortar compound to be tested in each case. Thethreaded rod was pushed in by hand. The excess mortar was removed usinga spatula.

The curing time in test 1 was 4 hours at 25° C. In test 2, the curingtime was 24 hours at 25° C.

The failure load was determined by centrally pulling out the threadedanchor rod with close support. The load values obtained with the mortarcompounds using a curing agent component (B) according to examples 1 to4 and comparative examples 1 to 5 are shown in table 10 below.

TABLE 10 Determination of the load values Examples Comparative examples1 2 3 4 1 2 3 4 5 Pull-out tests Test number Load value [N/mm²]  4 hcuring 1 31.1 29.1 7.4 24.6 25.8 18.9 1.7 0.4 17.9 24 h curing 2 34.438.8 35.5 35.0 37.3 38.2 36.5 36.8 36.1

1-15. (canceled)
 16. A method, comprising: accelerating an epoxy resincompound by combining the epoxy resin compound with at least one salt(S) comprising at least one salt of trifluoromethanesulfonic acid. 17.The method according to claim 16, wherein the epoxy resin compound is amulticomponent epoxy resin compound.
 18. The method according to claim17, wherein the multi-component epoxy resin compound comprises an epoxyresin component (A) which contains at least one curable epoxy resin, anda curing agent component (B) which contains at least one amine which isreactive to epoxy groups, and wherein the epoxy resin component (A) andthe curing agent component (B) are separate from one another so as toprevent a reaction.
 19. The method according to claim 18, wherein priorto combining, the multi-component epoxy resin compound is present incartridges or film pouches which comprise two or more separate chambersin which the epoxy resin component (A) and the curing agent component(B) are separately arranged so as to prevent the reaction.
 20. Themethod according to claim 16, further comprising: chemical fastening bycuring with the epoxy resin compound of a construction element oranchoring means in a borehole.
 21. The method according to claim 16,wherein the at least one salt (S) is Ca(CF₃SO₃)₂, Mg(CF₃SO₃)₂, orLi(CF₃SO₃)₂.
 22. The method according to claim 16, wherein the at leastone salt (S) comprises a cation selected from the group consisting ofalkali metals, alkaline earth metals, lanthanides, aluminum, ammonium,and combinations thereof.
 23. The method according to claim 18, whereinthe at least one amine reactive to epoxy groups is selected from thegroup consisting of 3-aminomethyl-3,5,5-trimethylcyclohexane (IPDA),2-methyl-1,5-pentanediamine, m-xylylenediamine (mXDA),1,3-bis(aminomethyl)-cyclohexane (1,3-BAC),4,4′-methylenebis(cyclohexyl-amine) (PACM),4-methylcyclohexyl-1,3-diamine (mCDA), 1,2-diaminocyclohexane (1,2-BAC),and mixtures thereof.
 24. The method according to claim 18, wherein theat least one salt (S) is present at least in the curing agent component(B).
 25. The method according to claim 16, wherein the at least one salt(S) is present in the epoxy resin compound in a proportion of from 0.1to 4 wt. %, based on a total weight of the epoxy resin compound.
 26. Themethod according to claim 18, wherein the at least one curable epoxyresin is a diglycidyl ether of bisphenol A or bisphenol F or a mixturethereof.
 27. A method for the chemical fastening of a construction meansand/or an anchoring material, the method comprising: chemical fasteningof the construction means and/or anchoring material with amulti-component epoxy resin compound which comprises an epoxy resincomponent (A) which contains at least one curable epoxy resin, and acuring agent component (B) which contains at least one amine which isreactive to epoxy groups, wherein the epoxy resin component (A) and thecuring agent component (B) are separate from one another so as toprevent a reaction, and then combined to cure, and wherein the epoxyresin component (A) and/or the curing agent component (B) comprises atleast one salt (S) as an accelerator, and wherein the at least one salt(S) comprises at least one salt of trifluoromethanesulfonic acid. 28.The method according to claim 27, wherein the multi-component epoxyresin compound, before being combined, is present in cartridges or filmpouches which comprise two or more separate chambers in which the epoxyresin component (A) and the curing agent component (B) are separatelyarranged so as to prevent the reaction.
 29. The method according toclaim 28, further comprising: discharging out of the two or moreseparate chambers and mixing in a static mixer or dissolver the epoxyresin component (A) and the curing agent component (B).
 30. The methodaccording to claim 29, further comprising: introducing a mixedmulti-component epoxy resin compound into a borehole.
 31. The methodaccording to claim 16, further comprising: chemical fastening by curingwith the epoxy resin compound.
 32. The method according to claim 16,further comprising: chemical fastening by curing with the epoxy resincompound of an anchor rod, anchor bolt, rod, threaded rod, sleeve,threaded sleeve, reinforcing bar, and/or screw in a borehole.
 33. Acomposition, comprising: an epoxy resin compound and at least one salt(S) comprising at least one salt of trifluoromethanesulfonic acid.